510(k) K900835 ยท LFJ Catheter, Subclavian
MODIFIED PERM-CATH
| Applicant | Quinton, Inc., Bothell WA, US |
| Decision | Substantially Equivalent, May 9, 1990 |
| Received | Feb 22, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900835
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.